Peer-reviewed veterinary case report
Congenital tail tumor with immature tissue in a male Burmese cat
By Kegler, K et al.·Published in Journal of comparative pathology·2014·Department of Pathology, Germany·View original on PubMed →
PetCaseFinder translated the abstract of this peer-reviewed paper into plain English so pet owners can read it. We do not publish original research — every detail traces back to the citation above. How we work →
Original publication title: Feline coccygeal teratoma: immunohistochemical characterization of immature tissue components.
- Species:
- cat
Plain-English summary
A male Burmese cat was found to have a congenital teratoma, which is a type of tumor, located near the base of his tail. The mass was both solid and cystic and was discovered during a veterinary examination. After surgery to remove the tumor, the cat showed no signs of recurrence even a year later. This case highlights that while teratomas can contain immature tissue, they can be successfully treated with surgery.
People also search for: cat tail tumor · Burmese cat teratoma · cat surgery recovery · congenital tumor in cats
Abstract
Congenital teratomas arising in the coccygeal region have not been reported in domestic animals. This report describes a congenital coccygeal teratoma in a male Burmese cat. A round to oval expansile mass with solid and cystic areas was found ventral to the 5th to 7th caudal vertebrae. Microscopically, the tumour was composed of derivatives of all three primordial germ layers with neuroectodermal predominance. Immunohistochemical double labelling identified immature tissue components in combination with Sox2, a regulator of stem cell proliferation and differentiation. Few Sox2-positive cells co-expressed the neural crest stem cell markers vimentin and neurotrophin receptor p75(NTR). Not all Sox2- and p75(NTR)-positive cells expressed vimentin. An overlapping expression of vimentin-negative and Sox2-, p75(NTR)-positive cells and GFAP- and p75(NTR)-positive cells may indicate a transition stage from immature to mature non-myelinating Schwann cells. Periaxin-positive myelinating Schwann cells surrounding neurofilament-positive axons were observed. Sox2 was additionally expressed in immature odontogenic epithelial cells and in immature cells of endodermal origin. Sox2 was not observed in mature cells, with the exception of satellite glial cells and mucous glands. Despite the presence of immature tissue components, no recurrence was observed 1 year after surgical removal.
Find similar cases for your pet
PetCaseFinder finds other peer-reviewed reports of pets with the same symptoms, plus a plain-English summary of what was tried across them.
Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/25005671/